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Identification of LsPIN1 gene and its potential functions in rhizome turning of Leymus secalinus
BACKGROUND: Continuous tilling and the lateral growth of rhizomes confer rhizomatous grasses with the unique ability to laterally expand, migrate and resist disturbances. They play key roles especially in degraded grasslands, deserts, sand dunes, and other fragile ecological system. The rhizomatous...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9670609/ https://www.ncbi.nlm.nih.gov/pubmed/36384450 http://dx.doi.org/10.1186/s12864-022-08979-7 |
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author | Li, Jialin Li, Hongmei Yin, Ning Quan, Xiaoyan Wang, Wenbo Shan, Qiuli Wang, Siqi Bermudez, Ramon Santos He, Wenxing |
author_facet | Li, Jialin Li, Hongmei Yin, Ning Quan, Xiaoyan Wang, Wenbo Shan, Qiuli Wang, Siqi Bermudez, Ramon Santos He, Wenxing |
author_sort | Li, Jialin |
collection | PubMed |
description | BACKGROUND: Continuous tilling and the lateral growth of rhizomes confer rhizomatous grasses with the unique ability to laterally expand, migrate and resist disturbances. They play key roles especially in degraded grasslands, deserts, sand dunes, and other fragile ecological system. The rhizomatous plant Leymus secalinus has both rhizome buds and tiller buds that grow horizontally and upward at the ends of rhizome differentiation and elongation, respectively. The mechanisms of rhizome formation and differentiation in L. secalinus have not yet been clarified. RESULTS: In this study, we found that the content of gibberellin A3 (GA(3)) and indole-3-acetic acid (IAA) were significantly higher in upward rhizome tips than in horizontal rhizome tips; by contrast, the content of methyl jasmonate and brassinolide were significantly higher in horizontal rhizome tips than in upward rhizome tips. GA(3) and IAA could stimulate the formation and turning of rhizomes. An auxin efflux carrier gene, LsPIN1, was identified from L. secalinus based on previous transcriptome data. The conserved domains of LsPIN1 and the relationship of LsPIN1 with PIN1 genes from other plants were analyzed. Subcellular localization analysis revealed that LsPIN1 was localized to the plasma membrane. The length of the primary roots (PRs) and the number of lateral roots (LRs) were higher in Arabidopsis thaliana plants overexpressing LsPIN1 than in wild-type (Col-0) plants. Auxin transport was altered and the gravitropic response and phototropic response were stronger in 35S:LsPIN1 transgenic plants compared with Col-0 plants. It also promoted auxin accumulation in root tips. CONCLUSION: Our findings indicated that LsPIN1 plays key roles in auxin transport and root development. Generally, our results provide new insights into the regulatory mechanisms underlying rhizome development in L. secalinus. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08979-7. |
format | Online Article Text |
id | pubmed-9670609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-96706092022-11-18 Identification of LsPIN1 gene and its potential functions in rhizome turning of Leymus secalinus Li, Jialin Li, Hongmei Yin, Ning Quan, Xiaoyan Wang, Wenbo Shan, Qiuli Wang, Siqi Bermudez, Ramon Santos He, Wenxing BMC Genomics Research BACKGROUND: Continuous tilling and the lateral growth of rhizomes confer rhizomatous grasses with the unique ability to laterally expand, migrate and resist disturbances. They play key roles especially in degraded grasslands, deserts, sand dunes, and other fragile ecological system. The rhizomatous plant Leymus secalinus has both rhizome buds and tiller buds that grow horizontally and upward at the ends of rhizome differentiation and elongation, respectively. The mechanisms of rhizome formation and differentiation in L. secalinus have not yet been clarified. RESULTS: In this study, we found that the content of gibberellin A3 (GA(3)) and indole-3-acetic acid (IAA) were significantly higher in upward rhizome tips than in horizontal rhizome tips; by contrast, the content of methyl jasmonate and brassinolide were significantly higher in horizontal rhizome tips than in upward rhizome tips. GA(3) and IAA could stimulate the formation and turning of rhizomes. An auxin efflux carrier gene, LsPIN1, was identified from L. secalinus based on previous transcriptome data. The conserved domains of LsPIN1 and the relationship of LsPIN1 with PIN1 genes from other plants were analyzed. Subcellular localization analysis revealed that LsPIN1 was localized to the plasma membrane. The length of the primary roots (PRs) and the number of lateral roots (LRs) were higher in Arabidopsis thaliana plants overexpressing LsPIN1 than in wild-type (Col-0) plants. Auxin transport was altered and the gravitropic response and phototropic response were stronger in 35S:LsPIN1 transgenic plants compared with Col-0 plants. It also promoted auxin accumulation in root tips. CONCLUSION: Our findings indicated that LsPIN1 plays key roles in auxin transport and root development. Generally, our results provide new insights into the regulatory mechanisms underlying rhizome development in L. secalinus. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08979-7. BioMed Central 2022-11-16 /pmc/articles/PMC9670609/ /pubmed/36384450 http://dx.doi.org/10.1186/s12864-022-08979-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Li, Jialin Li, Hongmei Yin, Ning Quan, Xiaoyan Wang, Wenbo Shan, Qiuli Wang, Siqi Bermudez, Ramon Santos He, Wenxing Identification of LsPIN1 gene and its potential functions in rhizome turning of Leymus secalinus |
title | Identification of LsPIN1 gene and its potential functions in rhizome turning of Leymus secalinus |
title_full | Identification of LsPIN1 gene and its potential functions in rhizome turning of Leymus secalinus |
title_fullStr | Identification of LsPIN1 gene and its potential functions in rhizome turning of Leymus secalinus |
title_full_unstemmed | Identification of LsPIN1 gene and its potential functions in rhizome turning of Leymus secalinus |
title_short | Identification of LsPIN1 gene and its potential functions in rhizome turning of Leymus secalinus |
title_sort | identification of lspin1 gene and its potential functions in rhizome turning of leymus secalinus |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9670609/ https://www.ncbi.nlm.nih.gov/pubmed/36384450 http://dx.doi.org/10.1186/s12864-022-08979-7 |
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